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Tagamet (Cimetidine) - Side Effect Reports to FDA

 
 



This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Tagamet (Cimetidine) and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.

Reports by Event Outcome

All Cases (27)
Life Threatening Events (2)
Disability (2)

Reports by Reaction Type

Drug Ineffective (8)Abnormal Dreams (2)Dialysis (2)Abortion Missed (2)Panic Reaction (2)Renal Failure Acute (2)Cerebrovascular Accident (2)Renal Impairment (2)Cerebral Infarction (2)Hemiplegia (2)Confusional State (1)Hypersensitivity (1)

Possible Tagamet side effects in female

Reported by a consumer/non-health professional from United States on 2012-08-17

Patient: female

Reactions: Flatulence

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in female

Reported by a consumer/non-health professional from United States on 2012-08-17

Patient: female

Reactions: Adverse Event

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 67 year old female

Reported by a consumer/non-health professional from United States on 2012-08-17

Patient: 67 year old female

Reactions: Drug Ineffective

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 48 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-17

Patient: 48 year old female

Reactions: Off Label Use, Pancreatic Disorder, Renal Impairment, Drug Ineffective, Abdominal Distension, Constipation

Drug(s) suspected as cause:
Tagamet
    Administration route: Oral
    Indication: Constipation

Unknown



Possible Tagamet side effects in female

Reported by a consumer/non-health professional from United States on 2012-08-17

Patient: female

Reactions: Dizziness

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 59 year old female

Reported by a consumer/non-health professional from United States on 2012-08-17

Patient: 59 year old female

Reactions: Faeces Pale

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 77 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-17

Patient: 77 year old female

Reactions: Drug Ineffective

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 37 year old male

Reported by a consumer/non-health professional from United States on 2012-08-17

Patient: 37 year old male

Reactions: Dyspnoea, Palpitations, Chest Pain

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 63 year old female

Reported by a consumer/non-health professional from United States on 2012-08-17

Patient: 63 year old female

Reactions: Hypersensitivity

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in male

Reported by a consumer/non-health professional from United States on 2012-08-17

Patient: male

Reactions: Abdominal Discomfort, Diarrhoea

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 65 year old female

Reported by a consumer/non-health professional from United States on 2012-08-17

Patient: 65 year old female

Reactions: Drug Ineffective

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 37 year old female

Reported by a consumer/non-health professional from United States on 2012-08-17

Patient: 37 year old female

Reactions: Drug Ineffective

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 57 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-17

Patient: 57 year old female

Reactions: Drug Ineffective

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 68 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-17

Patient: 68 year old female

Reactions: Drug Ineffective

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 58 year old female

Reported by a consumer/non-health professional from France on 2012-06-28

Patient: 58 year old female, weighing 78.0 kg (171.6 pounds)

Reactions: Pancreatitis Acute, Eosinophilia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Irbesartan
    Administration route: Oral
    Indication: Hypertension

Tagamet
    Indication: Premedication
    Start date: 2012-04-27

Metformin HCL
    Administration route: Oral
    Indication: Type 2 Diabetes Mellitus
    Start date: 2007-01-01



Possible Tagamet side effects in male

Reported by a consumer/non-health professional from United States on 2012-06-27

Patient: male

Reactions: Abnormal Dreams, Hallucination, Tactile, Panic Reaction

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 31 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2012-06-19

Patient: 31 year old female

Reactions: Dialysis, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Bupivacaine Aguettant
    Dosage: 10 mg, qd
    Indication: Spinal Anaesthesia
    Start date: 2012-01-08
    End date: 2012-01-08

Cefazolin
    Dosage: once daily
    Indication: Antibiotic Prophylaxis
    Start date: 2012-01-08
    End date: 2012-01-08

Clottafact
    Dosage: 6 g, qd
    Indication: Third Stage Postpartum Haemorrhage
    Start date: 2012-01-08
    End date: 2012-01-08

Sevoflurane
    Dosage: unk
    Indication: Anaesthesia
    Start date: 2012-01-08
    End date: 2012-01-08

Novoseven
    Dosage: 4 mg, qd
    Indication: Third Stage Postpartum Haemorrhage
    Start date: 2012-01-08
    End date: 2012-01-08

Ephedrine
    Dosage: 60 mg, qd
    Indication: Spinal Anaesthesia
    Start date: 2012-01-08
    End date: 2012-01-08

Tagamet
    Dosage: 400 mg, qd
    Indication: Spinal Anaesthesia
    Start date: 2012-01-08
    End date: 2012-01-08

Pabal
    Dosage: 100 a?g, qd
    Indication: Uterine Atony
    Start date: 2012-01-08
    End date: 2012-01-08

Nalador
    Dosage: 1000 a?g, qd
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-01-08
    End date: 2012-01-08

Omeprazole
    Dosage: 4 g, qd
    Indication: Postpartum Haemorrhage
    Start date: 2012-01-08
    End date: 2012-01-08

Other drugs received by patient: Platelets, Concentrated; RED Blood Cells; Celocurine / 00057702 /; Diprivan; Phenylephrine HCL; Voluven; Fresh Frozen Plasma; Tracrium



Possible Tagamet side effects in 31 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2012-06-07

Patient: 31 year old female

Reactions: Dialysis, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Novoseven
    Dosage: 4 mg, qd
    Indication: Third Stage Postpartum Haemorrhage
    Start date: 2012-01-08
    End date: 2012-01-08

Cefazolin
    Dosage: once daily
    Indication: Antibiotic Prophylaxis
    Start date: 2012-01-08
    End date: 2012-01-08

Ephedrine
    Dosage: 60 mg, qd
    Indication: Spinal Anaesthesia
    Start date: 2012-01-08
    End date: 2012-01-08

Omeprazole
    Dosage: 4 g, qd
    Indication: Postpartum Haemorrhage
    Start date: 2012-01-08
    End date: 2012-01-08

Tagamet
    Dosage: 400 mg, qd
    Indication: Spinal Anaesthesia
    Start date: 2012-01-08
    End date: 2012-01-08

Marcaine HCL
    Dosage: 10 mg, qd
    Indication: Spinal Anaesthesia

Sevoflurane
    Dosage: unk
    Indication: Anaesthesia
    Start date: 2012-01-08
    End date: 2012-01-08

Clottafact
    Dosage: 6 g, qd
    Indication: Third Stage Postpartum Haemorrhage
    Start date: 2012-01-08
    End date: 2012-01-08

Nalador
    Dosage: 1000 a?g, qd
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-01-08
    End date: 2012-01-08

Pabal
    Dosage: 100 a?g, qd
    Indication: Uterine Atony
    Start date: 2012-01-08
    End date: 2012-01-08

Other drugs received by patient: Celocurine / 00057702 /; Tracrium; Phenylephrine HCL; Fresh Frozen Plasma; Diprivan; RED Blood Cells; Voluven; Platelets, Concentrated



Possible Tagamet side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-05-11

Patient: female, weighing 50.8 kg (111.8 pounds)

Reactions: Confusional State, Tinnitus, Thinking Abnormal, Communication Disorder, Impaired Work Ability, Toxicity To Various Agents, Cognitive Disorder

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Tagamet
    Dosage: 200 mg every 12 hours po
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2012-04-17
    End date: 2012-04-30

Tagamet
    Dosage: 200 mg every 12 hours po
    Administration route: Oral
    Indication: Dyspepsia
    Start date: 2012-04-17
    End date: 2012-04-30



Possible Tagamet side effects in male

Reported by a consumer/non-health professional from United States on 2012-05-09

Patient: male

Reactions: Abnormal Dreams, Hallucination, Visual, Panic Reaction

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in female

Reported by a physician from United States on 2012-04-30

Patient: female

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
E-Mycin
    Dosage: unk

Paxil
    Dosage: unk

Biaxin
    Dosage: unk

Tagamet
    Dosage: unk

Nexium
    Dosage: unk

Gabapentin
    Dosage: unk

Celexa
    Dosage: unk



Possible Tagamet side effects in 35 year old female

Reported by a physician from Japan on 2012-03-16

Patient: 35 year old female

Reactions: Abortion Missed

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Prednisolone
    Dosage: 30 mg, 1x/day
    Administration route: Oral
    Start date: 2007-08-17
    End date: 2007-12-06

Prednisolone
    Dosage: 20 mg, 1x/day
    Administration route: Oral
    Start date: 2008-07-12

ONE-Alpha
    Dosage: 0.5 ug, 1x/day
    Administration route: Oral

Losartan Potassium
    Dosage: 50 mg, 1x/day
    Administration route: Oral
    Start date: 2008-03-05
    End date: 2009-09-11

Remicade
    Dosage: 200 mg, 1x/day
    Administration route: Oral
    Start date: 2008-03-14
    End date: 2008-03-14

Lipitor
    Dosage: 10 mg, 1x/day
    Administration route: Oral
    Start date: 2009-09-12

Losartan Potassium
    Dosage: 25 mg, 1x/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2008-03-04

Lipitor
    Dosage: 5 mg, 1x/day
    Administration route: Oral
    Indication: Hyperlipidaemia
    End date: 2009-09-11

Prograf
    Dosage: 3 mg, 1x/day
    Start date: 2007-05-31

Remicade
    Dosage: 200 mg, 1x/day
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2008-02-29
    End date: 2008-02-29

Prednisolone
    Dosage: 10-20 mg, alternate day
    Administration route: Oral
    Indication: Lupus Nephritis
    End date: 2007-08-16

Prednisolone
    Dosage: 30 mg, 1x/day
    Administration route: Oral
    Start date: 2008-01-05
    End date: 2008-05-09

Isoniazid
    Dosage: 300 mg, 1x/day
    Administration route: Oral
    Indication: Prophylaxis
    Start date: 2008-02-29
    End date: 2008-07-11

Prograf
    Dosage: 2 mg, 1x/day
    Indication: Lupus Nephritis
    Start date: 2007-04-19
    End date: 2007-05-30

Prednisolone
    Dosage: 25 mg, 1x/day
    Administration route: Oral
    Start date: 2007-12-07
    End date: 2008-01-04

Prednisolone
    Dosage: 25 mg, 1x/day
    Administration route: Oral
    Start date: 2008-05-09
    End date: 2008-07-11

Tagamet
    Dosage: 200 mg, 1x/day
    Administration route: Oral
    End date: 2008-03-09

Remicade
    Dosage: 200 mg, 1x/day
    Administration route: Oral
    Start date: 2008-04-10
    End date: 2008-04-10

Other drugs received by patient: Prednisolone; Prednisolone; Losartan Potassium and Hydrochlorothiazide; Prednisolone; Prednisolone; Losartan Potassium and Hydrochlorothiazide; Prednisolone; Prednisolone; Prednisolone



Possible Tagamet side effects in 35 year old female

Reported by a physician from Japan on 2012-03-13

Patient: 35 year old female, weighing 60.0 kg (132.0 pounds)

Reactions: Increased Appetite, Drug Ineffective, Abortion Missed, Blood Cholesterol Increased, Muscle Spasms, White Blood Cell Count Decreased, Blood Pressure Increased, Maternal Exposure During Pregnancy, Condition Aggravated, Glucose Urine Present, Irritability, Immunosuppressant Drug Level Decreased, Renal Impairment, Systemic Lupus Erythematosus, Lupus Nephritis, Platelet Count Decreased, Pregnancy

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Tacrolimus
    Dosage: 3 mg, unknown/d, oral; 2 mg, unknown/d, oral
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2007-04-19
    End date: 2007-05-30

Tacrolimus
    Dosage: 3 mg, unknown/d, oral; 2 mg, unknown/d, oral
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2007-05-31

Losartan Potassium
    Dosage: 25 mg, unknown/d, oral; 50 mg, unknown/d, oral
    Administration route: Oral
    Start date: 2008-03-05
    End date: 2009-09-11

Losartan Potassium
    Dosage: 25 mg, unknown/d, oral; 50 mg, unknown/d, oral
    Administration route: Oral
    End date: 2008-03-04

ONE-Alpha (Alfacalcidol) PER Oral NOS
    Dosage: 0.5 ug, unknown/d, oral
    Administration route: Oral

Lipitor
    Dosage: 5 mg, unknown/d, oral; 10 mg, unknown/d, oral
    Administration route: Oral
    Start date: 2011-09-12

Lipitor
    Dosage: 5 mg, unknown/d, oral; 10 mg, unknown/d, oral
    Administration route: Oral
    End date: 2009-09-11

Tagamet
    Dosage: 200 mg, unknown/d, oral
    Administration route: Oral
    End date: 2008-03-09

Isoniazid
    Dosage: 300 mg, unknown/d, oral
    Administration route: Oral
    Start date: 2008-02-29
    End date: 2008-07-11

Remicade
    Dosage: 200 mg, unknown/d, oral; 200 mg, unknown/d, oral
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2008-03-14

Remicade
    Dosage: 200 mg, unknown/d, oral; 200 mg, unknown/d, oral
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2008-04-10

Remicade
    Dosage: 200 mg, unknown/d, oral
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2008-02-29

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2009-02-13
    End date: 2009-08-07

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2009-10-10
    End date: 2009-11-06

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    End date: 2007-08-16

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2007-08-17
    End date: 2007-12-06

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2008-01-05
    End date: 2008-05-08

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2008-05-09
    End date: 2008-07-11

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2007-12-07
    End date: 2008-01-04

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2008-07-12
    End date: 2009-02-12

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2009-08-08
    End date: 2009-10-09

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2009-11-07
    End date: 2010-01-15

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2010-01-16
    End date: 2010-04-02

Prednisolone
    Dosage: see image
    Administration route: Oral
    Indication: Lupus Nephritis
    Start date: 2010-04-03

Other drugs received by patient: Losartan Potassium and Hydrochlorothiazide



Possible Tagamet side effects in 38 year old male

Reported by a health professional (non-physician/pharmacist) from United States on 2011-11-23

Patient: 38 year old male, weighing 68.0 kg (149.7 pounds)

Reactions: Product Quality Issue

Drug(s) suspected as cause:
Tagamet



Possible Tagamet side effects in 77 year old male

Reported by a physician from Japan on 2011-11-15

Patient: 77 year old male

Reactions: Renal Failure Chronic

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Rapaflo
    Dosage: 4 mg, daily
    Administration route: Oral
    Indication: Dysuria
    Start date: 2008-02-12
    End date: 2010-10-25

Krestin
    Dosage: unk
    Indication: Gastric Cancer

Tagamet
    Dosage: unk
    Administration route: Oral
    Indication: Gastric Cancer

UFT
    Dosage: unk
    Administration route: Oral
    Indication: Gastric Cancer



Possible Tagamet side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2011-11-04

Patient: female

Reactions: Cerebral Infarction, Hemiplegia, Cerebrovascular Accident

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Synthroid
    Dosage: 88 mg daily
    Indication: Thyroid Disorder

Tasigna
    Dosage: 400 mg, bid
    Administration route: Oral
    Indication: Chronic Myeloid Leukaemia
    Start date: 2011-01-01

Labetalol HCL
    Dosage: 100 mg, bid
    Indication: Hypertension

Tagamet
    Dosage: 200 mg, bid
    Indication: Gastrooesophageal Reflux Disease

Glyburide
    Dosage: 5 mg, bid
    Indication: Type 2 Diabetes Mellitus

Ciprofloxacin

Aspirin
    Dosage: unk

Tasigna
    Dosage: 200 mg, bid
    Administration route: Oral
    Start date: 2011-04-21



Possible Tagamet side effects in female

Reported by a individual with unspecified qualification from United States on 2011-11-04

Patient: female

Reactions: Cerebral Infarction, Hemiplegia, Cerebrovascular Accident

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Synthroid
    Dosage: 88 mg daily
    Indication: Thyroid Disorder

Glyburide
    Dosage: 5 mg, bid
    Indication: Type 2 Diabetes Mellitus

Tasigna
    Dosage: 400 mg, bid
    Administration route: Oral
    Indication: Chronic Myeloid Leukaemia
    Start date: 2011-01-01

Labetalol HCL
    Dosage: 100 mg, bid
    Indication: Hypertension

Ciprofloxacin

Tasigna
    Dosage: 200 mg, bid
    Administration route: Oral
    Start date: 2011-04-21

Aspirin
    Dosage: unk

Tagamet
    Dosage: 200 mg, bid
    Indication: Gastrooesophageal Reflux Disease

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